2-((tert-Butoxycarbonyl)amino)bicyclo[2.2.1]heptane-2-carboxylic acid
95%
- Product Code: 41187
CAS:
172927-01-4
| Molecular Weight: | 255.3101 g./mol | Molecular Formula: | C₁₃H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD25132076 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs and other bioactive compounds. The tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step synthetic processes. Its bicyclo[2.2.1]heptane structure contributes to the rigidity and stability of the resulting compounds, which is beneficial in drug design for targeting specific biological pathways. Additionally, it finds application in the synthesis of chiral compounds, where its unique structure aids in achieving high enantioselectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,080.00 |
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2-((tert-Butoxycarbonyl)amino)bicyclo[2.2.1]heptane-2-carboxylic acid
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs and other bioactive compounds. The tert-butoxycarbonyl (Boc) group acts as a protective group for amines, ensuring selective reactions during multi-step synthetic processes. Its bicyclo[2.2.1]heptane structure contributes to the rigidity and stability of the resulting compounds, which is beneficial in drug design for targeting specific biological pathways. Additionally, it finds application in the synthesis of chiral compounds, where its unique structure aids in achieving high enantioselectivity.
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